JPH08304971A - 多色ネガ写真要素 - Google Patents

多色ネガ写真要素

Info

Publication number: JPH08304971A
Authority: JP; Japan
Prior art keywords: coupler; layer; exposure; blue; dye
Prior art date: 1995-04-28
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP8107764A

Other languages

English (en)

Japanese (ja)

Inventor

Stephen P Singer

ポールシンガースティーブン

Paul Barrett Merkel

バレットメーケルポール

Jeffrey Walter Schmoeger

ウォルタースクモーガージェフリー

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-04-28

Filing date

1996-04-26

Publication date

1996-11-22

1996-04-26 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1996-11-22 Publication of JPH08304971A publication Critical patent/JPH08304971A/ja

Status Pending legal-status Critical Current

Links

-1 silver halide Chemical class 0.000 claims abstract description 81
239000000839 emulsion Substances 0.000 claims abstract description 31
238000010521 absorption reaction Methods 0.000 claims abstract description 17
229910052709 silver Inorganic materials 0.000 claims abstract description 16
239000004332 silver Substances 0.000 claims abstract description 16
238000012937 correction Methods 0.000 claims description 40
238000012545 processing Methods 0.000 abstract description 15
230000001235 sensitizing effect Effects 0.000 abstract description 13
239000000049 pigment Substances 0.000 abstract 2
239000001056 green pigment Substances 0.000 abstract 1
239000007800 oxidant agent Substances 0.000 abstract 1
230000001590 oxidative effect Effects 0.000 abstract 1
239000010410 layer Substances 0.000 description 50
239000000975 dye Substances 0.000 description 36
108010010803 Gelatin Proteins 0.000 description 15
229920000159 gelatin Polymers 0.000 description 15
239000008273 gelatin Substances 0.000 description 15
235000019322 gelatine Nutrition 0.000 description 15
235000011852 gelatine desserts Nutrition 0.000 description 15
230000000052 comparative effect Effects 0.000 description 14
238000011161 development Methods 0.000 description 14
238000000034 method Methods 0.000 description 14
239000000203 mixture Substances 0.000 description 11
230000007935 neutral effect Effects 0.000 description 11
230000035945 sensitivity Effects 0.000 description 10
239000000126 substance Substances 0.000 description 10
229910052740 iodine Inorganic materials 0.000 description 9
239000000463 material Substances 0.000 description 9
230000004044 response Effects 0.000 description 9
125000001424 substituent group Chemical group 0.000 description 9
229910052757 nitrogen Inorganic materials 0.000 description 8
238000011160 research Methods 0.000 description 8
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 8
239000011248 coating agent Substances 0.000 description 6
238000000576 coating method Methods 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 5
INVVMIXYILXINW-UHFFFAOYSA-N 5-methyl-1h-[1,2,4]triazolo[1,5-a]pyrimidin-7-one Chemical compound CC1=CC(=O)N2NC=NC2=N1 INVVMIXYILXINW-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
102100023705 C-C motif chemokine 14 Human genes 0.000 description 4
101000978381 Homo sapiens C-C motif chemokine 14 Proteins 0.000 description 4
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
239000003086 colorant Substances 0.000 description 4
230000006870 function Effects 0.000 description 4
230000008569 process Effects 0.000 description 4
238000004061 bleaching Methods 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
239000003112 inhibitor Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
239000004848 polyfunctional curative Substances 0.000 description 3
239000002356 single layer Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 2
206010070834 Sensitisation Diseases 0.000 description 2
230000002776 aggregation Effects 0.000 description 2
238000004220 aggregation Methods 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical compound CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
230000008859 change Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000009472 formulation Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
230000000873 masking effect Effects 0.000 description 2
239000006224 matting agent Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
230000008313 sensitization Effects 0.000 description 2
230000003595 spectral effect Effects 0.000 description 2
229960002317 succinimide Drugs 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
125000004149 thio group Chemical group *S* 0.000 description 2
GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
ILKZXYARHQNMEF-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-methoxyethyl)azanium;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1.CC1=CC=C(S(O)(=O)=O)C=C1.COCCN(CC)C1=CC=C(N)C(C)=C1 ILKZXYARHQNMEF-UHFFFAOYSA-N 0.000 description 1
IJHIIHORMWQZRQ-UHFFFAOYSA-N 1-(ethenylsulfonylmethylsulfonyl)ethene Chemical compound C=CS(=O)(=O)CS(=O)(=O)C=C IJHIIHORMWQZRQ-UHFFFAOYSA-N 0.000 description 1
SAVMNSHHXUMFRQ-UHFFFAOYSA-N 1-[bis(ethenylsulfonyl)methoxy-ethenylsulfonylmethyl]sulfonylethene Chemical compound C=CS(=O)(=O)C(S(=O)(=O)C=C)OC(S(=O)(=O)C=C)S(=O)(=O)C=C SAVMNSHHXUMFRQ-UHFFFAOYSA-N 0.000 description 1
RHMQDLNVMXZKHS-UHFFFAOYSA-N 2-[2-(4-amino-3-methylphenyl)ethylamino]ethanol Chemical compound CC1=CC(CCNCCO)=CC=C1N RHMQDLNVMXZKHS-UHFFFAOYSA-N 0.000 description 1
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 1
ORPXKVFCUSJGIS-UHFFFAOYSA-N 4-dodecylbenzenesulfonamide Chemical compound CCCCCCCCCCCCC1=CC=C(S(N)(=O)=O)C=C1 ORPXKVFCUSJGIS-UHFFFAOYSA-N 0.000 description 1
XTBFKMDOQMQYPP-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine;hydron;chloride Chemical compound Cl.CCN(CC)C1=CC=C(N)C=C1 XTBFKMDOQMQYPP-UHFFFAOYSA-N 0.000 description 1
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
AJDKZWLPPHJPOJ-UHFFFAOYSA-N C=1C=CC=C(Cl)C=1NN(CC)CC(C=1C=CC=CC=1)NC1=CC=CC=C1 Chemical compound C=1C=CC=C(Cl)C=1NN(CC)CC(C=1C=CC=CC=1)NC1=CC=CC=C1 AJDKZWLPPHJPOJ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
KKUKTXOBAWVSHC-UHFFFAOYSA-N Dimethylphosphate Chemical compound COP(O)(=O)OC KKUKTXOBAWVSHC-UHFFFAOYSA-N 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
235000009300 Ehretia acuminata Nutrition 0.000 description 1
244000046038 Ehretia acuminata Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
108091034117 Oligonucleotide Proteins 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000004904 UV filter Substances 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
MPLZNPZPPXERDA-UHFFFAOYSA-N [4-(diethylamino)-2-methylphenyl]azanium;chloride Chemical compound [Cl-].CC[NH+](CC)C1=CC=C(N)C(C)=C1 MPLZNPZPPXERDA-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 1
125000004744 butyloxycarbonyl group Chemical group 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
125000005521 carbonamide group Chemical group 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
229920006217 cellulose acetate butyrate Polymers 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000011247 coating layer Substances 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000007547 defect Effects 0.000 description 1
238000001739 density measurement Methods 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
XFUSKHPBJXJFRA-UHFFFAOYSA-N dihexyl hydrogen phosphite Chemical compound CCCCCCOP(O)OCCCCCC XFUSKHPBJXJFRA-UHFFFAOYSA-N 0.000 description 1
XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000012992 electron transfer agent Substances 0.000 description 1
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000010946 fine silver Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000005194 fractionation Methods 0.000 description 1
CRPAPNNHNVVYKL-UHFFFAOYSA-N hexadecane-1-sulfonamide Chemical compound CCCCCCCCCCCCCCCCS(N)(=O)=O CRPAPNNHNVVYKL-UHFFFAOYSA-N 0.000 description 1
AXSGBDGQLKZKQI-UHFFFAOYSA-N hexan-3-yl dihydrogen phosphate Chemical compound CCCC(CC)OP(O)(O)=O AXSGBDGQLKZKQI-UHFFFAOYSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
125000001841 imino group Chemical group [H]N=* 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000011229 interlayer Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
230000007774 longterm Effects 0.000 description 1
HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000003607 modifier Substances 0.000 description 1
QEALYLRSRQDCRA-UHFFFAOYSA-N myristamide Chemical compound CCCCCCCCCCCCCC(N)=O QEALYLRSRQDCRA-UHFFFAOYSA-N 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
KUWCVCMJPABJDI-UHFFFAOYSA-N n-[2-(4-amino-n-ethyl-3-methylanilino)ethyl]methanesulfonamide;sulfuric acid;dihydrate Chemical compound O.O.OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.CS(=O)(=O)NCCN(CC)C1=CC=C(N)C(C)=C1.CS(=O)(=O)NCCN(CC)C1=CC=C(N)C(C)=C1 KUWCVCMJPABJDI-UHFFFAOYSA-N 0.000 description 1
FECCTLUIZPFIRN-UHFFFAOYSA-N n-[2-[2-amino-5-(diethylamino)phenyl]ethyl]methanesulfonamide;hydrochloride Chemical compound Cl.CCN(CC)C1=CC=C(N)C(CCNS(C)(=O)=O)=C1 FECCTLUIZPFIRN-UHFFFAOYSA-N 0.000 description 1
QUBGMQIUQXZHBL-UHFFFAOYSA-N n-methyltetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NC QUBGMQIUQXZHBL-UHFFFAOYSA-N 0.000 description 1
AQJKSMHXNZWIGG-UHFFFAOYSA-N n-methyltetradecane-1-sulfonamide Chemical compound CCCCCCCCCCCCCCS(=O)(=O)NC AQJKSMHXNZWIGG-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000004989 p-phenylenediamines Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
125000006678 phenoxycarbonyl group Chemical group 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000002265 prevention Effects 0.000 description 1
238000003672 processing method Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000002798 spectrophotometry method Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
101150035983 str1 gene Proteins 0.000 description 1
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
239000011593 sulfur Chemical group 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
238000005406 washing Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000001043 yellow dye Substances 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/36—Couplers containing compounds with active methylene groups
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/3003—Materials characterised by the use of combinations of photographic compounds known as such, or by a particular location in the photographic element
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/3041—Materials with specific sensitometric characteristics, e.g. gamma, density
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
- G03C7/30511—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers characterised by the releasing group
- G03C7/30517—2-equivalent couplers, i.e. with a substitution on the coupling site being compulsory with the exception of halogen-substitution
- G03C7/30535—2-equivalent couplers, i.e. with a substitution on the coupling site being compulsory with the exception of halogen-substitution having the coupling site not in rings of cyclic compounds
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/3029—Materials characterised by a specific arrangement of layers, e.g. unit layers, or layers having a specific function
- G03C2007/3034—Unit layer
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/3029—Materials characterised by a specific arrangement of layers, e.g. unit layers, or layers having a specific function

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP8107764A 1995-04-28 1996-04-26 多色ネガ写真要素 Pending JPH08304971A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US43063995A	1995-04-28	1995-04-28
US430639		1995-04-28

Publications (1)

Publication Number	Publication Date
JPH08304971A true JPH08304971A (ja)	1996-11-22

Family

ID=23708411

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP8107764A Pending JPH08304971A (ja)	1995-04-28	1996-04-26	多色ネガ写真要素

Country Status (3)

Country	Link
US (1)	US5723263A (de)
EP (1)	EP0740202A3 (de)
JP (1)	JPH08304971A (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6406837B1 (en)	2000-09-18	2002-06-18	Eastman Kodak Company	Transparent imaging element with expanded color gamut
US6368759B1 (en)	2000-09-18	2002-04-09	Eastman Kodak Company	Display imaging element with expand color gamut
US6291144B1 (en)	2000-09-18	2001-09-18	Eastman Kodak Company	Day/night imaging member with expanded color gamut
US6368758B1 (en)	2000-09-18	2002-04-09	Eastman Kodak Company	Decorative package with expanded color gamut
US6465164B1 (en)	2000-09-18	2002-10-15	Eastman Kodak Company	Reflective imaging element with expanded color gamut

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1597510A1 (de) *	1967-12-21	1970-06-25	Agfa Gevaert Ag	Verbessertes farbphotographisches Material
JP2678827B2 (ja) *	1991-03-05	1997-11-19	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料
US5262292A (en) *	1991-04-23	1993-11-16	Eastman Kodak Company	Photographic elements containing pyrazolone couplers and process
US5391443A (en) *	1991-07-19	1995-02-21	Eastman Kodak Company	Process for the extraction of spectral image records from dye image forming photographic elements
US5447831A (en) *	1993-10-19	1995-09-05	Eastman Kodak Company	Photographic element employing hue correction couplers

1996
- 1996-04-24 EP EP96201097A patent/EP0740202A3/de not_active Ceased
- 1996-04-26 JP JP8107764A patent/JPH08304971A/ja active Pending
- 1996-11-12 US US08/748,067 patent/US5723263A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
EP0740202A2 (de)	1996-10-30
EP0740202A3 (de)	1997-03-12
US5723263A (en)	1998-03-03

Publication	Publication Date	Title
EP0740203B1 (de)	2003-03-26	Farb-Negativelement mit verbesserter Druckerverträglichkeit für die Grünaufzeichnung
US7629112B1 (en)	2009-12-08	Color photographic materials with yellow minimum density colorants
US6180328B1 (en)	2001-01-30	Photographic element for color imaging
US6197489B1 (en)	2001-03-06	Photographic element for color imaging
JPH08304971A (ja)	1996-11-22	多色ネガ写真要素
US6221571B1 (en)	2001-04-24	Silver halide light-sensitive element
US7632632B1 (en)	2009-12-15	Color photographic materials with magenta minimum density dyes
US5932407A (en)	1999-08-03	Color photographic element containing oxidized developer-scavenging naphtholic coupler forming wash-out dye
DE69723036T2 (de)	2004-05-06	Photographisches Element, das ein Redukton enthält und in der gegenüber blauem Licht am meisten empfindlichen Schicht eine feinkörnige Emulsion
EP0777149B1 (de)	2000-08-16	Photographische Elemente mit J-Aggregate bildenden, Infrarot-sensibilisierenden Carbocyaninfarbstoffen
US5719014A (en)	1998-02-17	Color negative films containing yellow methine dyes for filtration and density correction
EP0608958B1 (de)	2000-03-15	Photographisches Material und Verfahren beinhaltend ein Thiolbleichhilfsmittel in der geringstempfindlichen Schicht eines Dreischichtpakets
JPH07219167A (ja)	1995-08-18	多色写真要素
EP0740199B1 (de)	2003-01-22	Bestimmte Azoanilinfarben enthaltendes photographisches Element
EP0772081B1 (de)	2003-09-24	Dichtekorrekturfarbstoffe für Farbnegativfilme mit magnetischen Aufzeichnunsschichten
US6555304B1 (en)	2003-04-29	Direct view photographic element containing a particular red record
US6558886B1 (en)	2003-05-06	Direct view photographic element containing a particular green record
JPH07306506A (ja)	1995-11-21	写真要素
JPH07325373A (ja)	1995-12-12	写真要素
US6787297B1 (en)	2004-09-07	Dye-Layered silver halide photographic elements with low dye stain
US7101659B1 (en)	2006-09-05	Color photographic element with UV absorber
JP2004226978A (ja)	2004-08-12	ハロゲン化銀写真要素
JPH06295041A (ja)	1994-10-21	現像液の変化に対して改良されたレスポンスを有する写真要素
JPH1031281A (ja)	1998-02-03	改良された保存安定性を有するハロゲン化銀写真要素
EP0899612A1 (de)	1999-03-03	Abspaltverbindungen enthaltende photographische Elemente